65621-26-3Relevant articles and documents
Synthesis of (R)- and (S)-2,3-diaminopropyl sulfate: Mechanism based inhibition of glutamate 1-semialdehyde aminomutase
Khayer, Khurshida,Jenn, Thierry,Akhtar, Mahmoud,John, Robert,Gani, David
, p. 1637 - 1641 (2007/10/03)
A short synthesis of each enantiomer of 2,3-diaminopropyl hydrogensulfate is described starting from (2R)- and (2S)-asparagine. The compounds serve as inhibitors for pyridoxal 5'-phosphate-dependent (2S)- glutamate 1-semialdehyde aminotransferase, a target for selective herbicides and antibacterial agents on the tetrapyrrole biosynthetic pathway. The (2R)- enantiomer, as predicted, serves as a potent irreversible inactivator. (C) 2000 Elsevier Science Ltd.
AMIDE BOND ISOSTERES: IMIDAZOLINES IN PSEUDOPEPTIDE CHEMISTRY
Jones, Raymond C.F.,Ward, Gary J.
, p. 3853 - 3856 (2007/10/02)
The 2-imidazole ring has been incorporated as an amide bond replacement into pseudodipeptides, a pseudotripeptide, and pseudopentapeptide enkephalin analogues.